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| Data do envio | Título | Autor(s) |
|---|---|---|
| Ago-2012 | A case of severe hearing loss in action myoclonus renal failure syndrome resulting from mutation in SCARB2 | Perandones, Claudia ; Micheli, Federico E ; Pellene, Luis A ; Bayly, Marta A ; Berkovic, Samuel F ; Dibbens, Leanne M |
| Out-2004 | Acitretin embryopathy: a case report | Barbero, Pablo ; Lotersztein, Vanesa ; Bronberg, Rubén ; Perez, Miriam ; Alba, Liliana |
| 21-Out-2020 | GJB2 and GJB6 Genetic Variant Curation in an Argentinean Non-Syndromic Hearing-Impaired Cohort | Buonfiglio, Paula ; Bruque, Carlos D ; Luce, Leonela ; Giliberto, Florencia ; Lotersztein, Vanesa ; Menazzi, Sebastián ; Paoli, Bibiana ; Elgoyhen, Ana Belén ; Dalamón, Viviana |